المؤلفون: Shin'ichi Takeda, Mutsuki Kuraoka, Yoshitsugu Aoki

المصدر: Experimental Animals

مصطلحات موضوعية: 0301 basic medicine, Duchenne muscular dystrophy, Male, Pathology, medicine.medical_specialty, osteopontin, Review, Muscle disorder, Motor Activity, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, Dogs, Japan, Outcome Assessment, Health Care, medicine, accelerometry, X-linked muscular dystrophy, Animals, Humans, Osteopontin, Muscular dystrophy, General Veterinary, biology, outcome measure, business.industry, Muscle weakness, General Medicine, Young Investigator Award, medicine.disease, canine X-linked muscular dystrophy in Japan (CXMDJ), Gait, Muscular Dystrophy, Duchenne, Disease Models, Animal, 030104 developmental biology, biology.protein, Biomarker (medicine), Animal Science and Zoology, medicine.symptom, business, 030217 neurology & neurosurgery, Biomarkers

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::403a3075c7c2843f0178dbd0728fd88f
http://europepmc.org/articles/PMC8614006

المؤلفون: Bailey Miskew Nichols, author¹, Yoshitsugu Aoki, author², Mutsuki Kuraoka, author², Joshua J.A. Lee, author¹, Shin'ichi Takeda, author², Toshifumi Yokota, author¹

المصدر: Journal of Visualized Experiments. (111)

الإتاحة: http://www.jove.com/video/53776

المؤلفون: Tomoko Chiyo, Yuko Nitahara-Kasahara, Hiromi Hayashita-Kinoh, Mutsuki Kuraoka, Shin'ichi Takeda, Takashi Okada, Hironori Okada, Posadas-Herrera Guillermo

المصدر: Molecular Therapy: Methods & Clinical Development, Vol 20, Iss, Pp 133-141 (2021)
Molecular Therapy. Methods & Clinical Development

مصطلحات موضوعية: 0301 basic medicine, Pathology, medicine.medical_specialty, Stromal cell, lcsh:QH426-470, Duchenne muscular dystrophy, Transgene, viruses, microdystrophin, MSC, 03 medical and health sciences, 0302 clinical medicine, DMD, Genetics, medicine, X-linked muscular dystrophy, lcsh:QH573-671, Molecular Biology, Liver injury, DMD dog model, immune modulation, biology, business.industry, lcsh:Cytology, Mesenchymal stem cell, Neurotoxicity, AAV, medicine.disease, lcsh:Genetics, 030104 developmental biology, 030220 oncology & carcinogenesis, biology.protein, Molecular Medicine, Original Article, Dystrophin, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f27cdd7fae5823ace9af4578935a680
http://www.sciencedirect.com/science/article/pii/S2329050120302308

المؤلفون: Yoshitsugu Aoki, A Arzumanov, Kamel Mamchaoui, Tone Yuichiro, Rika Maruyama, Graham McClorey, Shin'ichi Takeda, Toshifumi Yokota, Yasumasa Hashimoto, Maria K. Tsoumpra, Michihiro Imamura, Vincent Mouly, Michael J. Gait, Matthew J.A. Wood, Reiko Terada

المساهمون: Gestionnaire, HAL Sorbonne Université 5, Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Centre de recherche en Myologie – U974 SU-INSERM, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), University of Alberta, University of Oxford, UMRS974, Université Pierre et Marie Curie - Paris 6 (UPMC), University of Oxford [Oxford], Institut de Myologie, Centre National de la Recherche Scientifique (CNRS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Association française contre les myopathies (AFM-Téléthon)-Sorbonne Université (SU), Centre de Recherche en Myologie

المصدر: Nucleic Acid Therapeutics
Nucleic Acid Therapeutics, 2021, 31 (2), pp.172-181. ⟨10.1089/nat.2020.0907⟩
Nucleic Acid Therapeutics, Mary Ann Liebert, Inc. publishers, 2021, 31 (2), pp.172-181. ⟨10.1089/nat.2020.0907⟩

مصطلحات موضوعية: 0301 basic medicine, canine X-linked muscular dystrophy in Japan (CXMD J ), Duchenne muscular dystrophy, Biochemistry, Morpholinos, Dystrophin, Myoblasts, Mice, 0302 clinical medicine, Drug Discovery, Muscular dystrophy, Telomerase, ComputingMilieux_MISCELLANEOUS, biology, Chemistry, Myogenesis, phosphorodiamidate morpholino oligomer, Exons, Original Papers, 3. Good health, Cell biology, 030220 oncology & carcinogenesis, Molecular Medicine, [SDV.MHEP.AHA] Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO], splice-switching oligonucleotides, Nonsense mutation, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, Cell Line, 03 medical and health sciences, Dogs, Genetics, medicine, [SDV.MHEP.AHA]Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO], Animals, Humans, Telomerase reverse transcriptase, Molecular Biology, Cyclin-Dependent Kinase 4, Genetic Therapy, immortalized dystrophic canine myoblast, Oligonucleotides, Antisense, canine X-linked muscular dystrophy in Japan (CXMDJ), medicine.disease, Exon skipping, Muscular Dystrophy, Duchenne, 030104 developmental biology, biology.protein, Cell-penetrating peptide, RNA Splice Sites, Peptides, cell-penetrating peptide

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37e6bb92dfaba5985c0590e408a2e368
https://hal.sorbonne-universite.fr/hal-03276095

المؤلفون: Paul Dowling, Maren Raucamp, Margit Zweyer, Sandra Murphy, Dieter Swandulla, Kay Ohlendieck

المصدر: Expert Review of Molecular Diagnostics. 19:739-755

مصطلحات موضوعية: Proteomics, 0301 basic medicine, Duchenne muscular dystrophy, Bioinformatics, Mass Spectrometry, Pathology and Forensic Medicine, Dystrophin, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, Protein Isoforms, X-linked muscular dystrophy, Muscular dystrophy, Muscle, Skeletal, Molecular Biology, biology, business.industry, Skeletal muscle, medicine.disease, Body Fluids, Muscular Dystrophy, Duchenne, 030104 developmental biology, medicine.anatomical_structure, Ion homeostasis, 030220 oncology & carcinogenesis, biology.protein, Molecular Medicine, Biomarker (medicine), business, Biomarkers

وصف الملف: text

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e236269315747b50b08de505a42bc663
https://doi.org/10.1080/14737159.2019.1648214

المؤلفون: Jean-Laurent Thibaud, Christophe Béroud, Adeline Vulin, Kevin M. Flanigan, Nicolas Wein, Nathalie Deburgrave, Stéphane Blot, Jean-Claude Kaplan, Isabel Punzón, Laurent Tiret, Cécile Peccate, Robert B. Weiss, Catherine Escriou, Inès Barthélémy, Nadège Calmels, Luis Garcia, Carole Drougard

المساهمون: Gestionnaire, Hal Sorbonne Université, Institut Mondor de Recherche Biomédicale (IMRB), Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), École nationale vétérinaire - Alfort (ENVA), Service de biochimie et de génétique moléculaire [CHU Cochin], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Cochin [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Laboratoire de Diagnostic Génétique [CHU Strasbourg], Université de Strasbourg (UNISTRA)-CHU Strasbourg, University of Utah School of Medicine [Salt Lake City], Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Ohio State University [Columbus] (OSU), Centre de recherche en Myologie – U974 SU-INSERM, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Institut de Myologie, Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Marseille medical genetics - Centre de génétique médicale de Marseille (MMG), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de Génétique Moléculaire [Hôpital de la Timone - APHM], Département de génétique médicale [Hôpital de la Timone - APHM], Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Handicap neuromusculaire : Physiopathologie, Biothérapie et Pharmacologies appliquées (END-ICAP), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut National de la Santé et de la Recherche Médicale (INSERM), École nationale vétérinaire d'Alfort (ENVA), Centre National de la Recherche Scientifique (CNRS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Association française contre les myopathies (AFM-Téléthon)-Sorbonne Université (SU), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU), Centre de Recherche en Myologie

المصدر: Skeletal Muscle
Skeletal Muscle, 2020, 10 (1), pp.23. ⟨10.1186/s13395-020-00239-0⟩
Skeletal Muscle, BioMed Central, 2020, 10 (1), pp.23. ⟨10.1186/s13395-020-00239-0⟩
Skeletal Muscle, Vol 10, Iss 1, Pp 1-22 (2020)

مصطلحات موضوعية: 0301 basic medicine, Male, lcsh:Diseases of the musculoskeletal system, Duchenne muscular dystrophy, [SDV]Life Sciences [q-bio], Canine, Dystrophin, 03 medical and health sciences, 0302 clinical medicine, Dogs, LRMD, DMD, medicine, Dog, X-linked muscular dystrophy, Animals, Orthopedics and Sports Medicine, Animal model, Disease-causing Mutation, Muscular dystrophy, Muscle, Skeletal, Molecular Biology, Gene, Genetics, Genes, Modifier, biology, Research, Inversion, Cell Biology, medicine.disease, Phenotype, 3. Good health, Muscular Dystrophy, Duchenne, [SDV] Life Sciences [q-bio], Disease Models, Animal, 030104 developmental biology, Mutation, biology.protein, Labrador Retriever, lcsh:RC925-935, Dp71, 030217 neurology & neurosurgery, Neuromuscular disorders

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3688323d713b671b97e2b41447f24486
https://hal.sorbonne-universite.fr/hal-02934725/document

المؤلفون: Cozzi, Francesca, Cerletti, Massimiliano, Luvoni, Gaia C., Lombardo, Rocco, Brambilla, Paola G., Faverzani, Stefano, Blasevich, Flavia, Cornelio, Ferdinando, Pozza, Ottaviano, Mora, Marina

المصدر: Acta Neuropathologica. May 2001 101(5):469-478

المؤلفون: Lanfossi, Massimo, Cozzi, Francesca, Bugini, Daniela, Colombo, Silvia, Scarpa, Paola, Morandi, Lucia, Galbiati, Silvia, Cornelio, Ferdinando, Pozza, Ottaviano, Mora, M.

المصدر: Acta Neuropathologica. January 1999 97(2):127-138

المساهمون: Lang, Florian, editor^Aff1

المصدر: Encyclopedia of Molecular Mechanisms of Disease. :2263-2263

المؤلفون: Eugenia Espinosa, Ana Isabel Sánchez, Nathalie Mariño, Andrés Felipe Araujo

المصدر: Repertorio de Medicina y Cirugía, Vol 28, Iss 2 (2019)
Repositorio Digital Institucional ReDi
Fundación Universitaria de Ciencias de la Salud-FUCS
instacron:Fundación Universitaria de Ciencias de la Salud-FUCS

مصطلحات موضوعية: 0301 basic medicine, Duchenne muscular dystrophy, Economics and Econometrics, Medicine (General), Duplication, Duplicación, 03 medical and health sciences, Exon, 0302 clinical medicine, R5-920, Dystrophinopathies, Gene duplication, Materials Chemistry, Media Technology, medicine, Distrofia muscular de Becker, Muscular dystrophy, Distrofinopatías, Gene, X chromosome, Genetics, business.industry, Point mutation, Forestry, medicine.disease, Phenotype, Distrofia muscular de Duchenne, 030104 developmental biology, X-linked muscular dystrophy, Becker, Distrofia muscular ligada a X, business, 030217 neurology & neurosurgery

وصف الملف: application/pdf; text/html; application/xml; application/epub+zip; audio/mpeg

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ead90a6051812462633f023efca1fce
https://revistas.fucsalud.edu.co/index.php/repertorio/article/view/920